JP7130312B2 - Adhesive tape - Google Patents

Adhesive tape Download PDF

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JP7130312B2
JP7130312B2 JP2019532251A JP2019532251A JP7130312B2 JP 7130312 B2 JP7130312 B2 JP 7130312B2 JP 2019532251 A JP2019532251 A JP 2019532251A JP 2019532251 A JP2019532251 A JP 2019532251A JP 7130312 B2 JP7130312 B2 JP 7130312B2
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pressure
adhesive tape
sensitive adhesive
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base material
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JPWO2019021371A1 (en
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靖史 土屋
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Teraoka Seisakusho Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22Plastics; Metallised plastics
    • C09J7/24Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/241Polyolefin, e.g.rubber
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J201/00Adhesives based on unspecified macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38Pressure-sensitive adhesives [PSA]
    • C09J7/381Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/385Acrylic polymers
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/10Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/12Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
    • C09J2301/122Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present only on one side of the carrier, e.g. single-sided adhesive tape
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/10Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
    • C09J2301/12Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
    • C09J2301/124Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present on both sides of the carrier, e.g. double-sided adhesive tape
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J2301/00Additional features of adhesives in the form of films or foils
    • C09J2301/30Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
    • C09J2301/312Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier parameters being the characterizing feature

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Adhesive Tapes (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

本発明は、加圧された場合の厚さの寸法安定性が優れ、例えばスマートフォン、タブレット端末等の電子機器、車載表示機、TV等の構造接着の用途において好適に使用できる粘着テープに関する。 TECHNICAL FIELD The present invention relates to a pressure-sensitive adhesive tape that has excellent dimensional stability of thickness when pressurized and can be suitably used for structural adhesion applications such as electronic devices such as smartphones and tablet terminals, vehicle-mounted displays, and TVs.

スマートフォン、タブレット端末等のポータブル電子機器は、一般にタッチパネルと液晶モジュールを収容する筐体を組み合わせた構造になっている。そして、例えばタッチパネルと筐体を固定する為に、粘着テープが用いられている。更に、車載表示機やTVの液晶ディスプレイ(LCD)パネル及び有機ELパネルと筐体を固定する為にも使用されている。 Portable electronic devices such as smartphones and tablet terminals generally have a structure in which a touch panel and a housing for housing a liquid crystal module are combined. For example, an adhesive tape is used to fix the touch panel and the housing. Furthermore, it is also used to fix the liquid crystal display (LCD) panel and the organic EL panel of the on-vehicle display device and the TV to the housing.

近年、これら電子機器の薄型化、小型化が進んでいる。これに伴い、例えばFPC(Flexible Printed Circuits)は機器内部でより鋭角に折り曲げられ、常時強い反発力がかかる内部構造になっている。また、LCDの表示領域をより大きくする為に液晶パネルを囲む枠(額縁)の幅を狭くする、いわゆる狭額縁化が進んでいる。したがって、筐体とトップパネルを固定する粘着テープも細幅化する必要がある。ただし内部からのFPC等の反発力や外部からの衝撃に耐える為には、粘着剤層の接着強度だけでなく、基材の強さも必要である。 In recent years, these electronic devices are becoming thinner and smaller. Along with this, FPCs (Flexible Printed Circuits), for example, are bent at a sharper angle inside the equipment, and have an internal structure that is always subjected to a strong repulsive force. Further, in order to increase the display area of the LCD, the width of the frame (frame) surrounding the liquid crystal panel is narrowed, that is, so-called frame narrowing is in progress. Therefore, it is necessary to narrow the width of the adhesive tape that secures the housing and the top panel. However, in order to withstand the repulsive force of the FPC and the like from the inside and the impact from the outside, not only the adhesive strength of the pressure-sensitive adhesive layer but also the strength of the substrate is required.

細幅の粘着テープを筐体に貼る際には、プレス機による加圧工程を実施することが一般的である。その際、粘着テープに掛かる圧力は0.1MPa~5.0MPaと広範囲に渡る。そして、その圧力範囲における粘着テープの厚さ変化が大きい場合は、図4(A)に示すように、両面粘着テープ41の寸法変化によってカバーパネル42と筐体43にギャップGが生じ、一体感が低下し、本来の外観が大幅に損なわれる。更に、圧力の変動による両面粘着テープ41の厚さ変化の差が大きい場合は、ギャップGを予測してカバーパネル42と筐体43を設計することは困難であり、設計自体が難しくなる。また、加圧工程後に時間の経過と共に両面粘着テープ41の寸法が復元する場合は、図4(B)に示すように、カバーパネル42が筐体43から飛び出し、落下時にカバーパネル42が破損する恐れがある。 When sticking a narrow adhesive tape to a housing, it is common to carry out a pressurizing process using a press machine. At that time, the pressure applied to the adhesive tape ranges from 0.1 MPa to 5.0 MPa. When the thickness of the adhesive tape varies greatly within that pressure range, the dimensional change of the double-sided adhesive tape 41 causes a gap G between the cover panel 42 and the housing 43, as shown in FIG. is reduced and the original appearance is greatly impaired. Furthermore, when the difference in thickness change of the double-sided adhesive tape 41 due to pressure fluctuation is large, it is difficult to predict the gap G and design the cover panel 42 and the housing 43, and the design itself becomes difficult. Further, when the dimensions of the double-sided adhesive tape 41 are restored with the lapse of time after the pressurizing process, as shown in FIG. There is fear.

ところで、この種の粘着テープの基材としては、ポリエチレンを主成分としたポリオレフィン系発泡体や、アクリル樹脂に様々なフィラーを添加したアクリルフォームを使用することが一般的である。例えば特許文献1には、発泡体基材の両面にアクリル系粘着剤層が設けられた両面粘着テープが記載されている。そして、この発泡体基材の具体例として、ポリエチレン発泡体、ポリプロピレン発泡体等のポリオレフィン系樹脂発泡体が記載されている。この発泡体基材の厚さは50~150μm、30%圧縮荷重は5~200kPaである。 By the way, as the base material of this type of pressure-sensitive adhesive tape, it is common to use a polyolefin foam containing polyethylene as a main component or an acrylic foam obtained by adding various fillers to an acrylic resin. For example, Patent Document 1 describes a double-sided pressure-sensitive adhesive tape in which acrylic pressure-sensitive adhesive layers are provided on both sides of a foam base material. Polyolefin resin foams such as polyethylene foams and polypropylene foams are described as specific examples of the foam base material. This foam substrate has a thickness of 50-150 μm and a 30% compressive load of 5-200 kPa.

特許文献2には、携帯電子機器の部品固定を目的とする、ポリオレフィン系発泡体基材と粘着剤層とからなる防水用両面粘着テープが記載されている。そして、このポリオレフィン系発泡体基材の厚さは70~300μm、25%圧縮強度は40~160kPa、引張強度は300~1500N/cm、厚さ方向の平均気泡径は1~100μm、流れ方向及び幅方向の平均気泡径は1.2~700μmである。Patent Literature 2 describes a waterproof double-sided adhesive tape composed of a polyolefin foam base material and an adhesive layer for the purpose of fixing parts of portable electronic devices. The polyolefin foam substrate has a thickness of 70 to 300 μm, a 25% compression strength of 40 to 160 kPa, a tensile strength of 300 to 1500 N/cm 2 , an average cell diameter in the thickness direction of 1 to 100 μm, and a flow direction. And the average cell diameter in the width direction is 1.2 to 700 μm.

特許文献3には、発泡体基材の少なくとも一面に粘着剤層を有する粘着テープが記載されている。そして、発泡体基材の具体例として、ポリエチレン、ポリプロピレン等のポリオレフィン系発泡体基材が記載されている。この発泡体基材の厚さは300μm以下、層間強度は6~50N/cm、25%圧縮強度は30kPa以上、引張強さは300N/cm以上、厚さ方向の平均気泡径は10~100μm、流れ方向及び幅方向の平均気泡径は10~700μmである。Patent Document 3 describes an adhesive tape having an adhesive layer on at least one surface of a foam substrate. As specific examples of foam substrates, polyolefin foam substrates such as polyethylene and polypropylene are described. The foam substrate has a thickness of 300 μm or less, an interlayer strength of 6 to 50 N/cm, a 25% compression strength of 30 kPa or more, a tensile strength of 300 N/cm 2 or more, and an average cell diameter in the thickness direction of 10 to 100 μm. , the average cell diameter in the machine direction and width direction is 10 to 700 μm.

特許文献4には、高い衝撃吸収性と静電気耐性を有する架橋ポリオレフィン系樹脂発泡シートが記載されている。この発泡シートの発泡倍率は1.1~2.8cm3/g、気泡のMDの平均気泡径は150~250μm、CDの平均気泡径は120~300μm、厚みは0.02~1.9mm、25%圧縮強度は250~1500kPaである。Patent Document 4 describes a crosslinked polyolefin resin foam sheet having high impact absorption and static resistance. The foamed sheet has an expansion ratio of 1.1 to 2.8 cm 3 /g, an MD average cell diameter of 150 to 250 μm, a CD average cell diameter of 120 to 300 μm, and a thickness of 0.02 to 1.9 mm. The 25% compressive strength is 250-1500 kPa.

特許文献5には、細幅化による性能低下が少ない粘着シートが記載されている。この粘着シートの100%モジュラスM[N/mm基材]と発泡体の密度D[g/cm]との関係は9.0≦(M/D)であり、100%モジュラスMは4.0[N/mm基材]よりも高い。Patent Literature 5 describes a pressure-sensitive adhesive sheet that is less likely to deteriorate in performance due to narrowing. The relationship between the 100% modulus M [N/mm 2 base material] of this adhesive sheet and the density D [g/cm 3 ] of the foam is 9.0≦(M/D), and the 100% modulus M is 4. higher than .0 [N/mm 2 substrate].

特許文献6には、携帯電子機器の表示部又は表示部保護材を筐体に固定する為の固定部材(発泡体基材を有する粘着テープ)が記載されている。この固定部材の細幅部の平均幅W[mm]と、固定部材の100%モジュラスM[N/mm基材]と、発泡体基材の厚さHs[mm]は、0.4/(M×Hs)≦Wの式を満たす。Patent Literature 6 describes a fixing member (adhesive tape having a foam base material) for fixing a display portion of a portable electronic device or a display portion protective material to a housing. The average width W [mm] of the narrow portion of the fixing member, the 100% modulus M [N/mm 2 base material] of the fixing member, and the thickness Hs [mm] of the foam base material are 0.4/ It satisfies the formula (M×Hs)≦W.

しかし特許文献1~6では、プレス機による加圧工程によるテープ厚さの変化とプレス工程後のテープ厚さの維持率に関しては十分検討されていない。さらに本発明者らの知見によれば、特許文献1~4に記載の従来の物性評価法では、その基材が細幅粘着テープに適するか否かを十分に評価できない。例えば、特許文献1~4に記載の「圧縮強度」又は「圧縮荷重」は単に厚さ方向の硬さの指標に過ぎず、圧縮後の厚さの変化に対する指標ではない。特許文献2及び3に記載の「引張強度」、「引張強さ」又は「層間強度」は、単に基材が破壊するときの強度である。特許文献3及び4に記載の「平均気泡径」又は「発泡倍率」は、発泡の程度を表す指標に過ぎない。特許文献5に記載の「100%モジュラス」は単にテープの引張強さを示すものである。特許文献6に記載の式「0.4/(M×Hs)≦W」は、単に引張強さとテープ厚さとテープ幅の関係式である。 However, in Patent Documents 1 to 6, the change in tape thickness due to the pressurizing process using a press machine and the retention rate of the tape thickness after the pressing process are not sufficiently studied. Furthermore, according to the findings of the present inventors, the conventional physical property evaluation methods described in Patent Documents 1 to 4 cannot sufficiently evaluate whether or not the substrate is suitable for a narrow pressure-sensitive adhesive tape. For example, the "compressive strength" or "compressive load" described in Patent Documents 1 to 4 are merely indices of hardness in the thickness direction, and are not indices of changes in thickness after compression. The "tensile strength", "tensile strength" or "interlaminar strength" described in Patent Documents 2 and 3 are simply the strength when the base material breaks. The "average cell diameter" or "expansion ratio" described in Patent Literatures 3 and 4 is merely an index representing the degree of foaming. The "100% modulus" described in Patent Document 5 simply indicates the tensile strength of the tape. The formula “0.4/(M×Hs)≦W” described in Patent Document 6 is simply a relational expression among tensile strength, tape thickness and tape width.

すなわち、特許文献1~6に記載の従来の物性評価法は、特に極細幅の粘着テープに対してそのまま適用することは必ずしも適当ではない。一方、本発明者らの知見によれば、極細幅の粘着テープを用いてカバーパネルと筐体をプレス機により加圧する工程においては、加圧後圧縮変形率が重要となり、さらに加圧後経時変形率の維持率、カバーガラスと筐体の剥れ難さにおいて、荷重-変位曲線における高荷重と低変位も重要となる。
That is, the conventional physical property evaluation methods described in Patent Documents 1 to 6 are not necessarily suitable to be applied as they are, especially to ultra-thin adhesive tapes. On the other hand, according to the knowledge of the present inventors, in the process of pressing the cover panel and the housing using a press machine using an ultra-thin adhesive tape, the compression deformation rate after pressing is important, and further pressing High load and low displacement in the load-displacement curve are also important for the maintenance rate of the post-time deformation rate and the difficulty of peeling of the cover glass and the housing.

特許第5947870号公報Japanese Patent No. 5947870 特許第4623198号公報Japanese Patent No. 4623198 特許第5517015号公報Japanese Patent No. 5517015 国際公開第2015/046526号WO2015/046526 特開2017-2292公報Japanese Patent Application Laid-Open No. 2017-2292 特開2017-2293公報Japanese Patent Application Laid-Open No. 2017-2293

本発明は、以上のような従来技術の課題を解決する為されたものである。すなわち、本発明の目的は、好ましくは極細幅の粘着テープであり、厚さの寸法安定性が優れ、例えばカバーパネルと筐体をプレスする工程等の加圧工程において生じるギャップGが小さく、ギャップGによる製品外観が損なわれ難く、また、製品の落下時のギャップGによる破損が生じ難い粘着テープを提供することにある。
The present invention has been made to solve the problems of the prior art as described above. That is, an object of the present invention is to provide an adhesive tape that preferably has an ultra-thin width, has excellent dimensional stability in thickness, and has a small gap G generated in a pressurizing process such as a process of pressing a cover panel and a housing. To provide an adhesive tape which hardly damages the appearance of a product due to the gap G, and hardly causes breakage due to the gap G when the product is dropped.

本発明者らは、上記目的を達成すべく鋭意検討した結果、特定の物性を示す基材を用いることが非常に有効であることを見出し、本発明を完成するに至った。 As a result of intensive studies aimed at achieving the above object, the inventors of the present invention have found that it is very effective to use a substrate exhibiting specific physical properties, and have completed the present invention.

すなわち本発明は、
基材の片面又は両面に粘着剤層を有する粘着テープであって、
前記基材がエチレン-酢酸ビニル共重合体と他のポリオレフィン系樹脂を含むポリオレフィン系樹脂組成物からなり、発泡倍率が1.1~3.5倍であり、かつ0.3mm~2.0mmのサイズのボイドを排除した発泡体であり、
前記基材がエチレン-酢酸ビニル共重合体を30質量%以上含み、
前記粘着剤層の厚さが、5~100μmであり、
前記粘着剤層が、(メタ)アクリル酸エステル共重合体架橋剤及びシランカップリング剤を含有するアクリル系粘着剤組成物を含み、前記(メタ)アクリル酸エステル共重合体を構成する単量体が、(メタ)アクリル酸アルキルエステル、カルボキシル基含有単量体及び水酸基含有単量体を含み、
前記粘着剤層が、前記(メタ)アクリル酸エステル共重合体に前記架橋剤を配合して形成した架橋構造を有し、
前記粘着テープの0.3~5.0MPaの範囲内で圧縮した際の接着時圧縮変形率が0~-10%である
ことを特徴とする粘着テープである。
That is, the present invention
An adhesive tape having an adhesive layer on one or both sides of a substrate,
The base material is made of a polyolefin resin composition containing an ethylene-vinyl acetate copolymer and other polyolefin resin, and has an expansion ratio of 1.1 to 3.5 times and an expansion ratio of 0.3 mm to 2.0 mm. It is a foam that eliminates voids of size,
The base material contains 30% by mass or more of an ethylene-vinyl acetate copolymer,
The pressure-sensitive adhesive layer has a thickness of 5 to 100 μm,
The adhesive layer comprises an acrylic adhesive composition containing a (meth)acrylic ester copolymer , a cross-linking agent and a silane coupling agent , and a monomer constituting the (meth)acrylic ester copolymer the body contains (meth)acrylic acid alkyl ester, a carboxyl group-containing monomer and a hydroxyl group-containing monomer,
The pressure-sensitive adhesive layer has a crosslinked structure formed by blending the (meth)acrylic acid ester copolymer with the crosslinking agent,
The pressure-sensitive adhesive tape is characterized by having a compressive deformation rate during adhesion of 0 to -10% when the pressure-sensitive adhesive tape is compressed within a range of 0.3 to 5.0 MPa.

先に述べた用途においては、一般に、独立気泡を含むポリエチレン系発泡基材が用いられる。圧縮強度が高い発泡基材と圧縮強度が低い発泡基材を比較すると、圧縮強度が低い発泡基材の方が圧力により大きく変形する。また、圧縮強度が高い発泡基材であっても、0.1~5.0MPaという非常に高い圧力で加圧すると、塑性変形により本来の厚さから大きく変化することがある。一方、本発明の粘着テープは、厚さの寸法安定性が優れ、例えばカバーパネルと筐体をプレスする工程等の加圧工程において生じるギャップGが小さく、ギャップGによる製品外観が損なわれ難く、また、製品の落下時のギャップGによる破損が生じ難い。したがって、そのような特性が必要な分野において、様々な用途に有用である。
In the applications mentioned above, polyethylene-based foam substrates containing closed cells are generally used. Comparing a foamed base material with high compressive strength and a foamed base material with low compressive strength, the foamed base material with low compressive strength deforms more under pressure. Moreover, even a foamed base material with high compressive strength may undergo a large change from its original thickness due to plastic deformation when pressurized with a very high pressure of 0.1 to 5.0 MPa. On the other hand, the pressure-sensitive adhesive tape of the present invention has excellent dimensional stability of thickness, and the gap G generated in the pressure process such as the process of pressing the cover panel and the housing is small, and the gap G does not impair the appearance of the product. Moreover, it is difficult for the product to be damaged due to the gap G when the product is dropped. Therefore, it is useful for various applications in fields where such properties are required.

実施例の曲げモーメントの測定方法を説明する為の模式的断面図である。FIG. 4 is a schematic cross-sectional view for explaining a bending moment measuring method of an example. 実施例の動的粘弾性測定により得られるマスターカーブを説明する為のグラフである。4 is a graph for explaining a master curve obtained by dynamic viscoelasticity measurement in Examples. 実施例の荷重-変位曲線の測定方法を説明する為の模式的断面図である。FIG. 4 is a schematic cross-sectional view for explaining a method for measuring a load-displacement curve in an example. 従来技術においてカバーパネルと筐体にギャップが生じる問題を説明する為の模式的断面図である。FIG. 10 is a schematic cross-sectional view for explaining a problem in which a gap is generated between the cover panel and the housing in the prior art;

<基材>
本発明に用いる基材は、この基材を有する粘着テープの0.3~5.0MPaの範囲内で圧縮した際の接着時圧縮変形率が0~-10%となる基材であれば良く、その種類は限定されない。例えば、エチレン-酢酸ビニル共重合体を30質量%以上含有し、且つ基材の引張弾性率が30N/mm以上である基材が好ましい。
<Base material>
The base material used in the present invention may be a base material having a compression deformation rate during adhesion of 0 to -10% when the pressure-sensitive adhesive tape having this base material is compressed within the range of 0.3 to 5.0 MPa. , the type of which is not limited. For example, a substrate containing 30% by mass or more of an ethylene-vinyl acetate copolymer and having a tensile modulus of elasticity of 30 N/mm 2 or more is preferable.

基材は、エチレン-酢酸ビニル共重合体と他のポリオレフィン系樹脂を含むポリオレフィン系樹脂組成物からなることが好ましい。他のポリオレフィン系樹脂としては、例えば、ポリエチレン系樹脂、ポリプロピレン系樹脂、又はこれらの混合物が挙げられる。特に、直鎖低密度ポリエチレン(LLDPE)や、エチレンプロピレンゴム(EPDM)が好ましい。 The substrate is preferably made of a polyolefin resin composition containing an ethylene-vinyl acetate copolymer and another polyolefin resin. Other polyolefin-based resins include, for example, polyethylene-based resins, polypropylene-based resins, or mixtures thereof. Linear low density polyethylene (LLDPE) and ethylene propylene rubber (EPDM) are particularly preferred.

基材を構成する樹脂組成物は、公知の方法により製造できる。例えば、エチレン-酢酸ビニル共重合体30質量%以上と他のポリオレフィン系樹脂を含有する樹脂組成物に電子線を照射して架橋させることにより、基材を構成する樹脂組成物が得られる。この架橋と同時又は異時に発泡させても良い。 The resin composition that constitutes the substrate can be produced by a known method. For example, a resin composition that constitutes the substrate can be obtained by irradiating a resin composition containing 30% by mass or more of an ethylene-vinyl acetate copolymer and another polyolefin resin with an electron beam to crosslink the resin composition. Foaming may be performed simultaneously with this cross-linking or at a different time.

基材を構成する樹脂組成物は、本発明の効果を損なわない範囲において他の添加剤を含んでいても良い。その具体例としては、増量剤、架橋剤、酸化防止剤、安定剤、エラストマー、カップリング剤が挙げられる。更に、遮光性フィラー、顔料を含んでいても良い。遮光性フィラーの具体例としては、カーボンブラック、カーボンナノチューブ、黒色無機フィラーが挙げられる。顔料の具体例としては、カーボンブラック、アニリンブラック、アセチレンブラック、ケッチェンブラックが挙げられる。 The resin composition constituting the base material may contain other additives as long as the effects of the present invention are not impaired. Specific examples thereof include extenders, cross-linking agents, antioxidants, stabilizers, elastomers and coupling agents. Furthermore, light shielding fillers and pigments may be included. Specific examples of light-shielding fillers include carbon black, carbon nanotubes, and black inorganic fillers. Specific examples of pigments include carbon black, aniline black, acetylene black, and ketjen black.

基材の幅は、好ましくは0.4~2.0mm、より好ましくは0.45~1.5mm、特に好ましくは0.6~1.2mmである。基材の厚さは、好ましくは0.05mm~1.0mm、より好ましくは0.05~0.4mmである。 The width of the substrate is preferably 0.4-2.0 mm, more preferably 0.45-1.5 mm, particularly preferably 0.6-1.2 mm. The thickness of the substrate is preferably 0.05-1.0 mm, more preferably 0.05-0.4 mm.

基材は発泡体であり、その発泡倍率は、好ましくは1.1~3.5倍、より好ましくは1.5~3.0倍である。発泡体の気泡形状は球状であることが好ましい。さらに基材が独立気泡を含むことは、防水性等の特性の点から好ましい。本発明においては、基材中に含まれるボイド径が0.3mm~2.0mmのサイズを排除するように管理した基材が好ましく、より好ましくは0.4mm~1.4mmのサイズを排除するように管理された基材であることが望ましい。また、管理された気泡径とは著しくサイズの異なるボイド(不良気泡)を含んでいない基材であることが好ましい。 The base material is a foam, and its expansion ratio is preferably 1.1 to 3.5 times, more preferably 1.5 to 3.0 times. The cell shape of the foam is preferably spherical. Furthermore, it is preferable that the base material contains closed cells from the viewpoint of properties such as waterproofness. In the present invention, it is preferable to use a substrate controlled so as to exclude void diameters of 0.3 mm to 2.0 mm contained in the substrate, and more preferably to exclude sizes of 0.4 mm to 1.4 mm. It is desirable that the base material is managed as follows. Moreover, it is preferable that the base material does not contain voids (defective cells) whose size is significantly different from the controlled cell diameter.

<粘着剤層>
本発明に用いる粘着剤層は特に限定されない。粘着剤層を構成する粘着剤組成物としては、例えばアクリル系、ゴム系、シリコーン系、ウレタン系等公知の様々な粘着剤組成物を使用できる。中でも、耐熱性、耐衝撃性、接着力、防水性の点からアクリル系粘着剤組成物が好ましく、粘着剤層は(メタ)アクリル酸エステル共重合体を含むことが好ましい。
<Adhesive layer>
The pressure-sensitive adhesive layer used in the present invention is not particularly limited. As the adhesive composition constituting the adhesive layer, various known adhesive compositions such as acrylic, rubber, silicone, and urethane can be used. Among them, an acrylic pressure-sensitive adhesive composition is preferable from the viewpoint of heat resistance, impact resistance, adhesive strength, and waterproofness, and the pressure-sensitive adhesive layer preferably contains a (meth)acrylic acid ester copolymer.

アクリル系粘着剤組成物の構成成分は特に限定されない。アクリル系粘着剤組成物は、通常、直鎖又は分岐鎖状のアルキル基を有する(メタ)アクリル酸アルキルエステルを単量体の主成分として用いて得られるアクリル系ポリマーを含む。(メタ)アクリル酸アルキルエステルの具体例としては、(メタ)アクリル酸メチル、(メタ)アクリル酸エチル、(メタ)アクリル酸プロピル、(メタ)アクリル酸イソプロピル、(メタ)アクリル酸ブチル、(メタ)アクリル酸イソブチル、(メタ)アクリル酸s-ブチル、(メタ)アクリル酸t-ブチル、(メタ)アクリル酸ペンチル、(メタ)アクリル酸イソペンチル、(メタ)アクリル酸ヘキシル、(メタ)アクリル酸ヘプチル、(メタ)アクリル酸オクチル、(メタ)アクリル酸2-エチルヘキシル、(メタ)アクリル酸イソオクチル、(メタ)アクリル酸ノニル、(メタ)アクリル酸イソノニル、(メタ)アクリル酸デシル、(メタ)アクリル酸イソデシル、(メタ)アクリル酸ウンデシル、(メタ)アクリル酸ドデシル、(メタ)アクリル酸トリデシル、(メタ)アクリル酸テトラデシル、(メタ)アクリル酸ペンタデシル、(メタ)アクリル酸ヘキサデシル、(メタ)アクリル酸ヘプタデシル、(メタ)アクリル酸オクタデシル、(メタ)アクリル酸ノナデシル、(メタ)アクリル酸エイコシル等の(メタ)アクリル酸C1-20アルキルエステルが挙げられる。中でも、(メタ)アクリル酸C2-14アルキルエステルが好ましく、(メタ)アクリル酸C2-10アルキルエステルがより好ましい。 The constituent components of the acrylic pressure-sensitive adhesive composition are not particularly limited. An acrylic pressure-sensitive adhesive composition usually contains an acrylic polymer obtained by using a (meth)acrylic acid alkyl ester having a linear or branched alkyl group as a main monomer component. Specific examples of (meth) acrylic acid alkyl esters include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, isopropyl (meth) acrylate, butyl (meth) acrylate, (meth) ) isobutyl acrylate, s-butyl (meth)acrylate, t-butyl (meth)acrylate, pentyl (meth)acrylate, isopentyl (meth)acrylate, hexyl (meth)acrylate, heptyl (meth)acrylate , octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, isooctyl (meth)acrylate, nonyl (meth)acrylate, isononyl (meth)acrylate, decyl (meth)acrylate, (meth)acrylic acid Isodecyl, undecyl (meth)acrylate, dodecyl (meth)acrylate, tridecyl (meth)acrylate, tetradecyl (meth)acrylate, pentadecyl (meth)acrylate, hexadecyl (meth)acrylate, heptadecyl (meth)acrylate , octadecyl (meth)acrylate, nonadecyl (meth)acrylate, and eicosyl (meth)acrylate. Among them, (meth)acrylic acid C2-14 alkyl ester is preferable, and (meth)acrylic acid C2-10 alkyl ester is more preferable.

アクリル系ポリマーを構成する単量体として、アクリル酸メチル等の(メタ)アクリル酸C1-3アルキルエステルを適当量用いることが好ましい。この(メタ)アクリル酸C1-3アルキルエステルは、狭額縁接着性、耐荷重性、加工性、狭額縁耐湿熱荷重性を向上する。(メタ)アクリル酸C1-3アルキルエステルの量は、アクリル系ポリマー100質量%中、好ましくは2質量%以上、より好ましくは3~15質量%である。この範囲の下限値は、狭額縁接着性、耐荷重性、加工性、狭額縁耐湿熱荷重性の点で意義がある。また上限値は、各種評価を実施する際の粘着テープの初期貼付け性の点で意義がある。 As a monomer constituting the acrylic polymer, it is preferable to use an appropriate amount of (meth)acrylic acid C1-3 alkyl ester such as methyl acrylate. This (meth)acrylic acid C1-3 alkyl ester improves narrow-frame adhesion, load resistance, processability, and narrow-frame wet heat load resistance. The amount of (meth)acrylic acid C1-3 alkyl ester is preferably 2% by mass or more, more preferably 3 to 15% by mass, based on 100% by mass of the acrylic polymer. The lower limit of this range is significant in terms of narrow-frame adhesion, load resistance, workability, and narrow-frame wet heat load resistance. Moreover, the upper limit value is significant in terms of the initial sticking property of the adhesive tape when performing various evaluations.

アクリル系ポリマーを構成する単量体として、接着力向上又は凝集力向上の為に、極性基含有単量体や多官能性単量体等の各種共重合性単量体を用いても良い。2種以上の共重合性単量体を組み合わせて用いても良い。更に、極性基含有単量体や多官能性単量体と反応し得る架橋剤を配合して架橋構造を形成させても良い。また、シランカップリング剤や酸化防止剤等の添加剤を配合しても良い。 As monomers constituting the acrylic polymer, various copolymerizable monomers such as polar group-containing monomers and polyfunctional monomers may be used in order to improve adhesion or cohesion. Two or more copolymerizable monomers may be used in combination. Furthermore, a cross-linking structure may be formed by blending a cross-linking agent capable of reacting with the polar group-containing monomer or the polyfunctional monomer. Additives such as silane coupling agents and antioxidants may also be blended.

極性基含有単量体の具体例としては、(メタ)アクリル酸、イタコン酸、マレイン酸、フマル酸、クロトン酸、イソクロトン酸等のカルボキシル基含有単量体又はその無水物(無水マレイン酸等);(メタ)アクリル酸ヒドロキシエチル、(メタ)アクリル酸ヒドロキシプロピル、(メタ)アクリル酸ヒドロキシブチル等の(メタ)アクリル酸ヒドロキシアルキル等の水酸基含有単量体;(メタ)アクリルアミド、N,N-ジメチル(メタ)アクリルアミド、N-メチロール(メタ)アクリルアミド、N-メトキシメチル(メタ)アクリルアミド、N-ブトキシメチル(メタ)アクリルアミド等のアミド基含有単量体;(メタ)アクリル酸アミノエチル、(メタ)アクリル酸ジメチルアミノエチル、(メタ)アクリル酸t-ブチルアミノエチル等のアミノ基含有単量体;(メタ)アクリル酸グリシジル、(メタ)アクリル酸メチルグリシジル等のグリシジル基含有単量体;(メタ)アクリロニトリル等のシアノ基含有単量体;N-ビニル-2-ピロリドン、(メタ)アクリロイルモルホリン、N-ビニルピリジン、N-ビニルピペリドン、N-ビニルピリミジン、N-ビニルピペラジン、N-ビニルピロール、N-ビニルイミダゾール、N-ビニルオキサゾール等の複素環含有ビニル系単量体;(メタ)アクリル酸メトキシエチル、(メタ)アクリル酸エトキシエチル等の(メタ)アクリル酸アルコキシアルキル系単量体;ビニルスルホン酸ナトリウム等のスルホン酸基含有単量体;2-ヒドロキシエチルアクリロイルフォスフェート等のリン酸基含有単量体;シクロヘキシルマレイミド、イソプロピルマレイミド等のイミド基含有単量体;2-メタクリロイルオキシエチルイソシアネート等のイソシアネート基含有単量体;が挙げられる。中でも、アクリル酸等のカルボキシル基含有単量体、アクリル酸ヒドロキシブチル等の水酸基含有単量体が好ましい。 Specific examples of polar group-containing monomers include carboxyl group-containing monomers such as (meth)acrylic acid, itaconic acid, maleic acid, fumaric acid, crotonic acid, and isocrotonic acid, or their anhydrides (maleic anhydride, etc.). ; hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, hydroxyl group-containing monomers such as hydroxyalkyl (meth) acrylate such as hydroxybutyl (meth) acrylate; (meth) acrylamide, N, N- Amide group-containing monomers such as dimethyl (meth) acrylamide, N-methylol (meth) acrylamide, N-methoxymethyl (meth) acrylamide, N-butoxymethyl (meth) acrylamide; (meth) aminoethyl acrylate, (meth ) amino group-containing monomers such as dimethylaminoethyl acrylate and t-butylaminoethyl (meth)acrylate; glycidyl group-containing monomers such as glycidyl (meth)acrylate and methylglycidyl (meth)acrylate; ( meth) cyano group-containing monomers such as acrylonitrile; heterocycle-containing vinyl monomers such as N-vinylimidazole and N-vinyloxazole; alkoxyalkyl (meth)acrylate monomers such as methoxyethyl (meth)acrylate and ethoxyethyl (meth)acrylate; vinyl sulfonic acid group-containing monomers such as sodium sulfonate; phosphoric acid group-containing monomers such as 2-hydroxyethyl acryloyl phosphate; imide group-containing monomers such as cyclohexylmaleimide and isopropylmaleimide; 2-methacryloyloxyethyl isocyanate and isocyanate group-containing monomers; Among them, carboxyl group-containing monomers such as acrylic acid and hydroxyl group-containing monomers such as hydroxybutyl acrylate are preferred.

カルボキシル基含有単量体は、狭額縁接着性、耐荷重性、加工性、狭額縁耐湿熱荷重性等の特性を向上する。カルボキシル基含有単量体の量は、アクリル系ポリマー100質量%中、好ましくは10~20質量%、より好ましくは10~12質量%である。これら範囲の下限値は、狭額縁接着性、耐荷重性、加工性、狭額縁耐湿熱荷重性の点で意義がある。また上限値は、各種評価を実施する際の粘着テープの初期貼付け性の点で意義がある。 A carboxyl group-containing monomer improves properties such as narrow-frame adhesion, load resistance, workability, and narrow-frame wet heat load resistance. The amount of the carboxyl group-containing monomer is preferably 10 to 20% by mass, more preferably 10 to 12% by mass, based on 100% by mass of the acrylic polymer. The lower limits of these ranges are significant in terms of tight-frame adhesion, load resistance, workability, and narrow-frame wet heat load resistance. Moreover, the upper limit value is significant in terms of the initial sticking property of the adhesive tape when performing various evaluations.

水酸基含有単量体は、狭額縁接着性、耐荷重性、加工性、狭額縁耐湿熱荷重性等の特性を向上する。水酸基含有単量体の量は、アクリル系ポリマー100質量%中、好ましくは0.01~2.0質量%、より好ましくは0.05~0.15質量%である。これら範囲の上限値は、粘着テープの加熱・湿熱雰囲気下での経時変化を抑制して、十分な狭額縁接着性、耐荷重性、加工性、狭額縁耐湿熱荷重等の特性を維持する点で意義がある。 A hydroxyl group-containing monomer improves properties such as narrow-frame adhesion, load resistance, workability, and narrow-frame wet heat load resistance. The amount of the hydroxyl group-containing monomer is preferably 0.01 to 2.0% by mass, more preferably 0.05 to 0.15% by mass, based on 100% by mass of the acrylic polymer. The upper limit of these ranges is to suppress the change over time of the adhesive tape in a heated/moist heat atmosphere, and to maintain sufficient narrow frame adhesion, load resistance, workability, narrow frame moist heat load resistance, etc. is meaningful.

粘着剤層の厚さは、好ましくは5~200μm、より好ましくは10~100μmである。 The thickness of the adhesive layer is preferably 5-200 μm, more preferably 10-100 μm.

粘着剤層は、例えば、粘着剤組成物を架橋反応させることにより形成できる。すなわち粘着剤組成物を基材上に塗布し、加熱により架橋反応させて基材上に粘着剤層を形成出来る。また、粘着剤組成物を離型紙又はその他のフィルム上に塗布し、加熱により架橋反応させて粘着剤層を形成し、この粘着剤層を基材の片面又は両面に貼り合せることも出来る。粘着剤組成物の塗布には、例えば、ロールコーター、ダイコーター、リップコーター等の塗布装置を使用できる。塗布後に加熱する場合は、加熱による架橋反応と共に粘着剤組成物中の溶剤も除去できる。なお、粘着剤層は粘着付与樹脂を含有しないことが好ましい。 The pressure-sensitive adhesive layer can be formed, for example, by subjecting the pressure-sensitive adhesive composition to a cross-linking reaction. That is, the pressure-sensitive adhesive composition can be coated on a substrate and crosslinked by heating to form a pressure-sensitive adhesive layer on the substrate. Alternatively, the adhesive composition may be coated on a release paper or other film, crosslinked by heating to form an adhesive layer, and the adhesive layer may be attached to one or both sides of a substrate. Coating devices such as roll coaters, die coaters, and lip coaters can be used to apply the adhesive composition. When heating after coating, the solvent in the pressure-sensitive adhesive composition can be removed together with the cross-linking reaction by heating. In addition, it is preferable that the adhesive layer does not contain a tackifying resin.

<粘着テープ>
本発明の粘着テープは、基材の片面又は両面に粘着剤層を有する。粘着剤層は基材の片面だけに形成しても良いが、両面に形成して両面粘着テープとすることが好ましい。
<Adhesive tape>
The pressure-sensitive adhesive tape of the present invention has a pressure-sensitive adhesive layer on one side or both sides of the substrate. The pressure-sensitive adhesive layer may be formed only on one side of the substrate, but is preferably formed on both sides to form a double-sided pressure-sensitive adhesive tape.

本発明の粘着テープの0.3~5.0MPaの範囲内で圧縮した際の接着時圧縮変形率は0~-10%であり、好ましくは0~-8%である。また、0.3~5.0MPaの範囲内で圧縮した後の接着時圧縮変形率の維持率は、好ましくは±3%以内、より好ましくは±2%以内である。 When the pressure-sensitive adhesive tape of the present invention is compressed within the range of 0.3 to 5.0 MPa, the compression deformation ratio during adhesion is 0 to -10%, preferably 0 to -8%. In addition, the rate of retention of compression deformation during bonding after compression within the range of 0.3 to 5.0 MPa is preferably within ±3%, more preferably within ±2%.

本発明の粘着テープは、最低損失正接が50~100℃の範囲内にあり、最低損失正接と150℃損失正接の差が1.5×10-1以下であることが好ましい。最低損失正接が50~100℃の範囲内にあることは、動的接着力と剥離変位の点で意義がある。また、最低損失正接と150℃損失正接の差が1.5×10-1以下であることは、接着時圧縮変形率と動的接着力と剥離変位の点で意義がある。The pressure-sensitive adhesive tape of the present invention preferably has a minimum loss tangent in the range of 50 to 100° C. and a difference between the minimum loss tangent and the 150° C. loss tangent of 1.5×10 −1 or less. A minimum loss tangent within the range of 50 to 100° C. is significant in terms of dynamic adhesive strength and peel displacement. In addition, the difference between the lowest loss tangent and the 150° C. loss tangent of 1.5×10 −1 or less is significant in terms of compression deformation rate during bonding, dynamic adhesive strength, and peel displacement.

本発明の粘着テープの貯蔵弾性率変化点αは、好ましくは100℃以上である。また、毎分1mmで引っ張った際の荷重-変位曲線において、基材の層間破壊がなく、最大荷重値が40N/cm以上であり、剥離変位が2.0mm以下であることが好ましい。The storage modulus change point α of the pressure-sensitive adhesive tape of the present invention is preferably 100° C. or higher. Further, in the load-displacement curve when the substrate is pulled at 1 mm/min, it is preferable that there is no delamination of the base material, the maximum load value is 40 N/cm 2 or more, and the peel displacement is 2.0 mm or less.

本発明の粘着テープのJIS K-7181に準じた圧縮強度測定で測定される40%圧縮強度は、好ましくは2MPa以上、より好ましくは2~5MPaである。 The pressure-sensitive adhesive tape of the present invention preferably has a 40% compression strength of 2 MPa or more, more preferably 2 to 5 MPa, as measured by compression strength measurement according to JIS K-7181.

以上説明した各物性値の具体的な測定条件は、後述する実施例に記載のとおりである。 Specific measurement conditions for each physical property value described above are as described in Examples described later.

本発明の粘着テープは、0.1~5.0MPaと非常に高い圧力でプレスすることが可能である。特に、その寸法安定性から細幅粘着テープに適している。したがって、そのような特性が必要な分野において様々な用途に有用である。具体的には、構造接着用粘着テープ、電子機器接着用粘着テープとして非常に有用である。 The pressure-sensitive adhesive tape of the present invention can be pressed at a very high pressure of 0.1-5.0 MPa. In particular, due to its dimensional stability, it is suitable for narrow adhesive tapes. Therefore, it is useful for various applications in fields where such properties are required. Specifically, it is very useful as a pressure-sensitive adhesive tape for bonding structures and a pressure-sensitive adhesive tape for bonding electronic devices.

以下、実施例及び比較例を挙げて、本発明を更に詳細に説明する。以下の記載において「部」は質量部、「%」は質量%を意味する。 EXAMPLES The present invention will now be described in more detail with reference to examples and comparative examples. In the following description, "parts" means parts by mass, and "%" means % by mass.

<粘着剤層の製造例1~3>
攪拌機、温度計、還流冷却器及び窒素ガス導入管を備えた反応装置に、表1に示す量(%)の成分(A1)~(A5)と、酢酸エチル、連鎖移動剤としてn-ドデカンチオール及び過酸化物系ラジカル重合開始剤としてラウリルパーオキサイド0.1部を仕込んだ。反応装置内に窒素ガスを封入し、攪拌しながら窒素ガス気流下で68℃、3時間、その後78℃、3時間で重合反応させた。次いで、室温まで冷却し、酢酸エチルを添加した。これにより、固形分濃度30%のアクリル系共重合体(A)を得た。
<Preparation Examples 1 to 3 of adhesive layer>
A reaction apparatus equipped with a stirrer, a thermometer, a reflux condenser and a nitrogen gas inlet tube was charged with the components (A1) to (A5) in the amounts (%) shown in Table 1, ethyl acetate, and n-dodecanethiol as a chain transfer agent. And 0.1 part of lauryl peroxide was charged as a peroxide radical polymerization initiator. Nitrogen gas was sealed in the reactor, and the polymerization reaction was carried out at 68° C. for 3 hours under a nitrogen gas stream with stirring, and then at 78° C. for 3 hours. It was then cooled to room temperature and ethyl acetate was added. As a result, an acrylic copolymer (A) having a solid concentration of 30% was obtained.

各アクリル系共重合体の重量平均分子量(Mw)及び理論Tgを表1に示す。この重量平均分子量(Mw)は、GPC法により、アクリル系共重合体の標準ポリスチレン換算の分子量を以下の測定装置及び条件にて測定した値である。
・装置:LC-2000シリーズ(日本分光株式会社製)
・カラム:Shodex KF-806M×2本、Shodex KF-802×1本
・溶離液:テトラヒドロフラン(THF)
・流速:1.0mL/分
・カラム温度:40℃
・注入量:100μL
・検出器:屈折率計(RI)
・測定サンプル:アクリル系ポリマーをTHFに溶解させ、アクリル系ポリマーの濃度が0.5質量%の溶液を作製し、フィルターによるろ過でゴミを除去したもの。
Table 1 shows the weight average molecular weight (Mw) and theoretical Tg of each acrylic copolymer. This weight average molecular weight (Mw) is a value obtained by measuring the molecular weight of the acrylic copolymer in terms of standard polystyrene by the GPC method using the following measuring apparatus and conditions.
・ Apparatus: LC-2000 series (manufactured by JASCO Corporation)
・Column: Shodex KF-806M x 2, Shodex KF-802 x 1 ・Eluent: Tetrahydrofuran (THF)
・Flow rate: 1.0 mL/min ・Column temperature: 40°C
・Injection volume: 100 μL
・Detector: Refractometer (RI)
・Measurement sample: An acrylic polymer was dissolved in THF to prepare a solution having an acrylic polymer concentration of 0.5% by mass, and dust was removed by filtration through a filter.

理論Tgは、FOXの式により算出した値である。 The theoretical Tg is a value calculated by the FOX formula.

Figure 0007130312000001
Figure 0007130312000001

表1中の略号は、以下の通りである。
「MA」:メチルアクリレート
「2-EHA」:2-エチルヘキシルアクリレート
「BA」:n-ブチルアクリレート
「AA」:アクリル酸
「4-HBA」:4-ヒドロキシブチルアクリレート
「Vac」:酢酸ビニル
Abbreviations in Table 1 are as follows.
"MA": methyl acrylate "2-EHA": 2-ethylhexyl acrylate "BA": n-butyl acrylate "AA": acrylic acid "4-HBA": 4-hydroxybutyl acrylate "Vac": vinyl acetate

そして、各アクリル系共重合体(A)の固形分100部に対し、架橋剤(B)として東ソー株式会社製のイソシアネート系架橋剤(コロネート(登録商標)L-45E、45%溶液)0.04部、シランカップリング剤(C)として信越化学工業社製のシランカップリング剤(商品名KBM-403)0.1部、酸化防止剤(D)としてBASF社製の酸化防止剤(イルガノックス(登録商標)1010)0.1部を加えて混合し、粘着剤組成物を調製した。次いで、110℃で溶媒を除去・乾燥すると共に架橋反応させて、粘着剤組成物をシリコーン処理された離型紙上に乾燥後の厚みが0.075mmになるように塗布した。 Then, to 100 parts of the solid content of each acrylic copolymer (A), 0.5% of an isocyanate cross-linking agent (Coronate (registered trademark) L-45E, 45% solution) manufactured by Tosoh Corporation is added as a cross-linking agent (B). 04 parts, 0.1 part of silane coupling agent (trade name KBM-403) manufactured by Shin-Etsu Chemical Co., Ltd. as silane coupling agent (C), antioxidant (D) BASF antioxidant (Irganox (registered trademark) 1010) was added and mixed to prepare an adhesive composition. Next, the solvent was removed and dried at 110° C., and cross-linking was allowed to occur, and the pressure-sensitive adhesive composition was applied onto silicone-treated release paper so as to have a thickness of 0.075 mm after drying.

<実施例1>
まず、エチレン-酢酸ビニル共重合体含むポリエチレン(PE)系発泡体からなる基材(厚さ=0.15mm、引張弾性率=46.1N/mm、曲げモーメント(MD方向)=16gf/cm、(TD方向)=17gf/cm、発泡倍率=1.9、密度=544kg/m)であって、ボイド(不良気泡)を含んでいない基材を用意した。そして、この基材の両面をコロナ放電処理し、基材の両面に製造例1で得た離型紙上の粘着剤層を貼り合せ、40℃で3日間養生して、両面粘着テープを得た。
<Example 1>
First, a base material made of polyethylene (PE) foam containing ethylene-vinyl acetate copolymer (thickness = 0.15 mm, tensile modulus = 46.1 N/mm 2 , bending moment (MD direction) = 16 gf/cm , (TD direction) = 17 gf/cm, expansion ratio = 1.9, density = 544 kg/m 3 ) and no voids (defective cells) were prepared. Then, both sides of this base material were subjected to corona discharge treatment, and the adhesive layer on the release paper obtained in Production Example 1 was attached to both sides of the base material, and cured at 40° C. for 3 days to obtain a double-sided adhesive tape. .

<実施例2及び3>
粘着剤層として、製造例2及び3で得た粘着剤層を使用したこと以外は、実施例1と同様にして両面粘着テープを得た。
<Examples 2 and 3>
A double-sided pressure-sensitive adhesive tape was obtained in the same manner as in Example 1, except that the pressure-sensitive adhesive layers obtained in Production Examples 2 and 3 were used as the pressure-sensitive adhesive layer.

<比較例1>
基材として、PE系発泡体(厚さ=0.2mm、引張弾性率=21.0N/mm、曲げモーメント(MD方向)=3gf/cm、(TD方向)=4gf/cm、発泡倍率=3、密度=330kg/m)を使用し、粘着剤層の乾燥後の厚みが0.05mmであること以外は、実施例1と同様にして両面粘着テープを得た。
<Comparative Example 1>
As a substrate, a PE-based foam (thickness = 0.2 mm, tensile modulus = 21.0 N/mm 2 , bending moment (MD direction) = 3 gf/cm, (TD direction) = 4 gf/cm, expansion ratio = 3, density = 330 kg/m 3 ), and a double-sided pressure-sensitive adhesive tape was obtained in the same manner as in Example 1 except that the thickness of the pressure-sensitive adhesive layer after drying was 0.05 mm.

<比較例2>
基材として、PE系発泡体(厚さ=0.15mm、引張弾性率=23.7N/mm、曲げモーメント(MD方向)=7gf/cm、(TD方向)=8gf/cm、発泡倍率=1.8、密度=560kg/m)を使用したこと以外は、実施例1と同様にして両面粘着テープを得た。
<Comparative Example 2>
As a base material, a PE-based foam (thickness = 0.15 mm, tensile modulus = 23.7 N/mm 2 , bending moment (MD direction) = 7 gf/cm, (TD direction) = 8 gf/cm, expansion ratio = 1.8, density = 560 kg/m 3 ) to obtain a double-sided pressure-sensitive adhesive tape in the same manner as in Example 1.

実施例及び比較例の基材の引張弾性率、並びに基材及び粘着テープの曲げモーメントは、以下の方法により測定した値である。各測定値を表2に示す。 The tensile elastic modulus of the base material and the bending moment of the base material and the adhesive tape in Examples and Comparative Examples are values measured by the following methods. Each measured value is shown in Table 2.

(引張弾性率)
基材を幅(W)10mm、長さ70mmの短冊状(長辺がMD方向)に裁断し、これを試験片とした。そして、厚さを1/100ダイヤルゲージ(N=5)で測定し、5点の平均値を厚さ(t)とし、以下の式から試験片の断面積(S)を求めた。
断面積S(mm)=t×W
t:厚さ(mm)
W:幅(mm)
(tensile modulus)
The base material was cut into a strip having a width (W) of 10 mm and a length of 70 mm (the long side is in the MD direction), and this was used as a test piece. Then, the thickness was measured with a 1/100 dial gauge (N=5), the average value of 5 points was taken as the thickness (t), and the cross-sectional area (S) of the test piece was obtained from the following formula.
Cross-sectional area S (mm 2 ) = t x W
t: thickness (mm)
W: Width (mm)

JIS K7161 2014に基づき、市販の引張試験装置(東洋精機製作所社製、装置名ストログラフV-10C、フルスケール50N)のチャック間隔(L)を20mmに設定し、試験片の上端及び下端をチャックした。その後、引張速度10mm/分で引張り、引張荷重-変位曲線を得た。得られた引張荷重-変位曲線の変位が0.05mm及び0.25mmの引張荷重から直線式を求めた。得られた直線式から引張荷重F=10Nの時の変位x(mm)を求め、下記の式より基材の腰の指標となる引張弾性率を求めた。
引張弾性率(N/mm)=(F/S)/(x/L)
F:引張荷重=10(N)
S:断面積(mm
x:引張荷重=10Nの時の変位(mm)
L:チャック間隔=20(mm)
Based on JIS K7161 2014, set the chuck interval (L) of a commercially available tensile tester (manufactured by Toyo Seiki Seisakusho, device name Strograph V-10C, full scale 50N) to 20 mm, and chuck the upper and lower ends of the test piece. did. Then, it was pulled at a tensile speed of 10 mm/min to obtain a tensile load-displacement curve. A linear equation was determined from the tensile load with a displacement of 0.05 mm and 0.25 mm in the resulting tensile load-displacement curve. A displacement x (mm) at a tensile load F=10 N was obtained from the obtained linear equation, and a tensile elastic modulus, which is an index of the stiffness of the base material, was obtained from the following equation.
Tensile modulus (N/mm 2 ) = (F/S)/(x/L)
F: Tensile load = 10 (N)
S: cross-sectional area (mm 2 )
x: Displacement (mm) when tensile load = 10 N
L: Chuck interval = 20 (mm)

なお、各直線式及び引張弾性率は以下の通りである。
実施例1~3:直線式 y=3.6667x+0.0767、引張弾性率 46.1N/mm
比較例1:直線式 y=1.2632x-0.0432、引張弾性率 21.0N/mm
比較例2:直線式 y=2.1026x+0.1349、引張弾性率 23.7N/mm
In addition, each linear equation and tensile elastic modulus are as follows.
Examples 1 to 3: Linear formula y = 3.6667x + 0.0767, tensile modulus 46.1 N / mm 2
Comparative Example 1: Linear formula y=1.2632x-0.0432, tensile modulus 21.0 N/mm 2
Comparative Example 2: Linear formula y = 2.1026x + 0.1349, tensile modulus 23.7 N / mm 2

(曲げモーメント)
基材(又は両面粘着テープ)11を幅38mm、長さ50mmの短冊状に裁断し、これを試験片とした。得られた試験片を図1に示すように4本の端子12に挟み込んだ。そして、JIS P8125に基づき、市販のテーバー剛性度試験機(東洋精機製作所社製)の試験時に稼働する部分に設置し、上下10gの重りを振り子へ取り付け、曲げ速度3°/sec、曲げ角度15°の時の目盛を読み、これを測定値とした。そして、この測定値を以下の計算式に代入し、MD方向及びTD方向の曲げモーメント(M)を算出した。
曲げモーメント(gf/cm)=38.0nk/w
n:目盛の読み(10gの重りの時は1)
k:一目盛当りのモーメント(gf/cm)
w:試験片の幅
(bending moment)
A substrate (or double-sided adhesive tape) 11 was cut into strips having a width of 38 mm and a length of 50 mm, which were used as test pieces. The obtained test piece was sandwiched between four terminals 12 as shown in FIG. Then, based on JIS P8125, a commercially available Taber stiffness tester (manufactured by Toyo Seiki Seisakusho Co., Ltd.) was installed at the part that operates during the test, a vertical 10 g weight was attached to the pendulum, and the bending speed was 3 ° / sec and the bending angle was 15. Read the scale in ° and use this as the measured value. Then, the measured values were substituted into the following formulas to calculate bending moments (M) in the MD and TD directions.
Bending moment (gf/cm) = 38.0 nk/w
n: Reading on the scale (1 when the weight is 10g)
k: Moment per scale (gf/cm)
w: Width of test piece

Figure 0007130312000002
Figure 0007130312000002

<評価試験>
実施例及び比較例で得た両面粘着テープを、以下の方法で評価した。結果を表3~6に示す。
<Evaluation test>
The double-sided pressure-sensitive adhesive tapes obtained in Examples and Comparative Examples were evaluated by the following methods. The results are shown in Tables 3-6.

(接着時圧縮変形率)
実施例及び比較例で得た両面粘着テープを、10mm×10mmの正方形状に加工し、厚さ75μmの白色PETフィルムで両側から挟み込み、プレス機にて加圧した。この際、粘着テープへ実際に加わる圧力が、0.3MPa、0.5MPa、1.0MPa、1.5MPa、2.0MPa、4.0MPa、5.0MPaとなる各条件で加圧した。この加圧後5分以内に、キーエンス社製レーザーマイクロスコープVK-X260にてテープ断面を観察し厚さを測定した。そして下記式により、接着時圧縮変形率を算出した。
(接着時圧縮変形率)=(加圧前の厚さ-加圧後の厚さ)/(加圧前の厚さ)×100[%]
(Compressive deformation rate during adhesion)
The double-sided pressure-sensitive adhesive tapes obtained in Examples and Comparative Examples were processed into squares of 10 mm×10 mm, sandwiched from both sides by white PET films having a thickness of 75 μm, and pressed with a press. At this time, the actual pressure applied to the adhesive tape was 0.3 MPa, 0.5 MPa, 1.0 MPa, 1.5 MPa, 2.0 MPa, 4.0 MPa, and 5.0 MPa. Within 5 minutes after this pressurization, the thickness of the tape was measured by observing the cross section of the tape with a laser microscope VK-X260 manufactured by Keyence Corporation. Then, the compressive deformation rate during adhesion was calculated by the following formula.
(Compressive deformation rate during adhesion) = (thickness before pressure - thickness after pressure) / (thickness before pressure) x 100 [%]

(接着時圧縮変形率の維持率)
接着時圧縮変形率を測定した各両面粘着テープを23℃、50%RH下にて24時間保存した。その後、キーエンス社製レーザーマイクロスコープVK-X260にてテープ断面を観察し厚さを測定した。そして下記式により、接着時圧縮変形率の維持率を算出した。
(接着時圧縮変形率の維持率)=(加圧後24時間保存した際の厚さ-加圧直後の厚さ)/(加圧直後の厚さ)×100[%]
(Maintenance rate of compressive deformation rate during bonding)
Each double-faced pressure-sensitive adhesive tape whose compressive deformation rate during adhesion was measured was stored at 23° C. and 50% RH for 24 hours. Then, the thickness of the tape was measured by observing the cross section of the tape with a laser microscope VK-X260 manufactured by Keyence Corporation. Then, the retention rate of the compressive deformation rate during bonding was calculated by the following formula.
(Maintenance rate of compression deformation rate during adhesion) = (thickness when stored for 24 hours after pressurization - thickness immediately after pressurization) / (thickness immediately after pressurization) x 100 [%]

(貯蔵弾性率変化点α、最低損失正接、150℃損失正接)
実施例及び比較例で得た両面粘着テープを、厚さが2mmになるまで重ね合せ、動的粘弾性測定装置(TAインスツルメントジャパン(株)製、RDA-III)を用いて、冶具はパラレルプレートφ8mm、周波数10Hz、測定温度-50℃~150℃、昇温速度10℃/分の条件で動的粘弾性を測定し、図2に示すようなマスターカーブを得、貯蔵弾性率変化点α、最低損失正接、150℃損失正接を得た。
(Storage modulus change point α, lowest loss tangent, 150°C loss tangent)
The double-sided adhesive tapes obtained in Examples and Comparative Examples were superimposed to a thickness of 2 mm, and a dynamic viscoelasticity measuring device (TA Instruments Japan Co., Ltd., RDA-III) was used to measure the jig. The dynamic viscoelasticity was measured under the conditions of a parallel plate of φ8 mm, a frequency of 10 Hz, a measurement temperature of -50° C. to 150° C., and a heating rate of 10° C./min to obtain a master curve as shown in FIG. α, lowest loss tangent, 150° C. loss tangent were obtained.

(荷重-変位曲線の最大荷重と変位)
実施例及び比較例で得た両面粘着テープを10mm×10mmのサイズに裁断し、一方の離型紙を剥離した。そして図3に示すように、SUS304製T字治具32に両面粘着テープ31を貼り合せ、次いでもう一方の離型紙を剥離し、長さ125mm、幅50mm、2.0mm厚のガラス板33に貼り合せた。0.5MPaで10秒間加圧し、その後5分以内に23℃、50%RHの雰囲気下で、上方向に1mm/分の速度で引張り、荷重-変位曲線を得た。得られた曲線から最大荷重と、貼り合せ部分がはがれた時の変位mmを測定した。
(maximum load and displacement of load-displacement curve)
The double-sided pressure-sensitive adhesive tapes obtained in Examples and Comparative Examples were cut into a size of 10 mm×10 mm, and the release paper on one side was peeled off. Then, as shown in FIG. 3, a T-shaped jig 32 made of SUS304 was pasted with a double-sided adhesive tape 31, and then the other release paper was peeled off. pasted together. A pressure of 0.5 MPa was applied for 10 seconds, followed by pulling upward at a rate of 1 mm/min in an atmosphere of 23° C. and 50% RH within 5 minutes to obtain a load-displacement curve. From the resulting curve, the maximum load and the displacement mm when the bonded portion was peeled off were measured.

(40%及び50%圧縮強度)
実施例及び比較例で得た両面粘着テープを、厚さが12mmになるまで重ね合せ、圧縮強度測定装置((株)島津製作所製、AG-20kNX)を用い、測定(解析)ソフトはトラペジウムX、測定モードはシングルの条件で、JIS K-7181に準じ0~50%の圧縮強度を測定し、マスターカーブを作成し、40%及び50%圧縮強度を得た。
(40% and 50% compressive strength)
The double-sided adhesive tapes obtained in Examples and Comparative Examples were superimposed to a thickness of 12 mm, and a compressive strength measuring device (manufactured by Shimadzu Corporation, AG-20kNX) was used, and measurement (analysis) software was Trapezium X. , under the condition of single measurement mode, 0 to 50% compressive strength was measured according to JIS K-7181, a master curve was created, and 40% and 50% compressive strengths were obtained.

Figure 0007130312000003
Figure 0007130312000003

Figure 0007130312000004
Figure 0007130312000004

Figure 0007130312000005
Figure 0007130312000005

<評価>
表3~6の評価結果から明らかなように、実施例1~3の両面粘着テープは、40%及び50%圧縮強度に関係なく全ての特性が優れていた。
<Evaluation>
As is clear from the evaluation results in Tables 3 to 6, the double-sided pressure-sensitive adhesive tapes of Examples 1 to 3 were excellent in all properties regardless of 40% and 50% compressive strength.

比較例1及び2の両面粘着テープは接着時圧縮変形率が大きいので、例えば図4(A)に示すように、加圧工程における両面粘着テープ41の厚さの寸法変化によってカバーパネル42と筐体43のギャップGが大きくなり、一体感が低下し、本来の外観が大幅に損なわれる恐れがある。また、比較例1及び2の両面粘着テープは0.1MPa~5.0MPaの各圧力における接着時圧縮変形率の差が大きいので、ギャップGを予測してカバーパネル42と筐体43を設計することは困難である。 Since the double-faced adhesive tapes of Comparative Examples 1 and 2 have a large compressive deformation ratio during adhesion, the cover panel 42 and the housing are separated from each other by a dimensional change in the thickness of the double-sided adhesive tape 41 in the pressure process, as shown in FIG. 4A, for example. The gap G between the bodies 43 becomes large, the sense of unity is lowered, and there is a possibility that the original appearance is greatly damaged. In addition, since the double-sided adhesive tapes of Comparative Examples 1 and 2 have a large difference in compression deformation rate during adhesion at each pressure of 0.1 MPa to 5.0 MPa, the cover panel 42 and the housing 43 are designed by estimating the gap G. is difficult.

比較例1の両面粘着テープは接着時圧縮変形率の維持率が大きい(変形を維持できない)ので、ギャップGを予測してカバーパネル42と筐体43を設計しても、例えば図4(B)に示すようにカバーパネル42が筐体43から飛び出してしまう恐れがある。 Since the double-sided adhesive tape of Comparative Example 1 has a large rate of maintaining the compressive deformation rate during adhesion (the deformation cannot be maintained), even if the gap G is predicted and the cover panel 42 and the housing 43 are designed, for example, FIG. ), the cover panel 42 may protrude from the housing 43 .

比較例1及び2の両面粘着テープは貯蔵弾性率変化点αが100℃以下なので、ギャップGを予測してカバーパネル42と筐体43を設計することがより困難である。また比較例1の両面粘着テープは引張力による荷重-変位曲線の最大荷重が低いので、引張り力によって剥がれ易い傾向にある。 Since the double-sided pressure-sensitive adhesive tapes of Comparative Examples 1 and 2 have a storage elastic modulus change point α of 100° C. or less, it is more difficult to predict the gap G and design the cover panel 42 and the housing 43 . Further, the double-sided pressure-sensitive adhesive tape of Comparative Example 1 has a low maximum load in the load-displacement curve due to tensile force, so it tends to be easily peeled off by tensile force.

本発明の粘着テープは、40%及び50%圧縮強度に関係なく接着時圧縮変形率が小さいので、そのような特性が必要な分野において、様々な用途に利用可能である。特にスマートフォン、タブレット端末等の電子機器の用途において好適に使用できる。具体的には、筐体とカバーパネルとの固定や車載用LCDと筐体の固定等に使用できる。 Since the pressure-sensitive adhesive tape of the present invention has a small compressive deformation rate during adhesion regardless of the compressive strength of 40% and 50%, it can be used in various fields where such properties are required. In particular, it can be suitably used for electronic devices such as smartphones and tablet terminals. Specifically, it can be used for fixing a housing and a cover panel, fixing a vehicle-mounted LCD and a housing, and the like.

11 基材(又は両面粘着テープ)
12 端子
31 両面粘着テープ
32 SUS304製T字治具
33 ガラス板
41 両面粘着テープ
42 カバーパネル
43 筐体
G ギャップ
11 base material (or double-sided adhesive tape)
12 terminal 31 double-sided adhesive tape 32 SUS304 T-shaped jig 33 glass plate 41 double-sided adhesive tape 42 cover panel 43 housing G gap

Claims (13)

基材の片面又は両面に粘着剤層を有する粘着テープであって、
前記基材がエチレン-酢酸ビニル共重合体と他のポリオレフィン系樹脂を含むポリオレフィン系樹脂組成物からなり、発泡倍率が1.1~3.5倍であり、かつ0.3mm~2.0mmのサイズのボイドを排除した発泡体であり、
前記基材がエチレン-酢酸ビニル共重合体を30質量%以上含み、
前記粘着剤層の厚さが、5~100μmであり、
前記粘着剤層が、(メタ)アクリル酸エステル共重合体架橋剤及びシランカップリング剤を含有するアクリル系粘着剤組成物を含み、前記(メタ)アクリル酸エステル共重合体を構成する単量体が、(メタ)アクリル酸アルキルエステル、カルボキシル基含有単量体及び水酸基含有単量体を含み、
前記粘着剤層が、前記(メタ)アクリル酸エステル共重合体に前記架橋剤を配合して形成した架橋構造を有し、
前記粘着テープの0.3~5.0MPaの範囲内で圧縮した際の接着時圧縮変形率が0~-10%である
ことを特徴とする粘着テープ。
An adhesive tape having an adhesive layer on one or both sides of a substrate,
The base material is made of a polyolefin resin composition containing an ethylene-vinyl acetate copolymer and other polyolefin resin, and has an expansion ratio of 1.1 to 3.5 times and an expansion ratio of 0.3 mm to 2.0 mm. It is a foam that eliminates voids of size,
The base material contains 30% by mass or more of an ethylene-vinyl acetate copolymer,
The thickness of the adhesive layer is 5 to100μm,
The pressure-sensitive adhesive layer is a (meth) acrylic acid ester copolymer,cross-linking agentand silane coupling agentwherein the monomers constituting the (meth)acrylic acid ester copolymer are (meth)acrylic acid alkyl ester, a carboxyl group-containing monomer and a hydroxyl group-containing monomer including
The pressure-sensitive adhesive layer has a crosslinked structure formed by blending the (meth)acrylic acid ester copolymer with the crosslinking agent,
When the pressure-sensitive adhesive tape is compressed within the range of 0.3 to 5.0 MPa, the compression deformation rate at the time of adhesion is 0 to -10%.
An adhesive tape characterized by:
0.3~5.0MPaの範囲内で圧縮した後の接着時圧縮変形率の維持率が±3%以内である請求項1記載の粘着テープ。 2. The pressure-sensitive adhesive tape according to claim 1, wherein the rate of retention of compression deformation during adhesion after compression within the range of 0.3 to 5.0 MPa is within ±3%. 最低損失正接が50~100℃の範囲内にあり、最低損失正接と150℃損失正接の差が1.5×10-1以下である請求項1記載の粘着テープ。 2. The pressure-sensitive adhesive tape according to claim 1, wherein the minimum loss tangent is in the range of 50 to 100° C., and the difference between the minimum loss tangent and the 150° C. loss tangent is 1.5×10 −1 or less. 貯蔵弾性率変化点αが100℃以上である請求項1記載の粘着テープ。 2. The pressure-sensitive adhesive tape according to claim 1, wherein the storage modulus change point α is 100° C. or higher. 前記基材が、球状の気泡を含む請求項1または4に記載の粘着テープ。 5. The pressure-sensitive adhesive tape according to claim 1, wherein the base material contains spherical air bubbles. 毎分1mmで引っ張った際の荷重-変位曲線において、基材の層間破壊がなく、最大荷重値が40N/cm以上であり、剥離変位が2.0mm以下である請求項1記載の粘着テープ。 2. The pressure-sensitive adhesive tape according to claim 1, wherein the load-displacement curve when pulled at 1 mm/min shows no interlaminar breakage of the base material, a maximum load value of 40 N/cm 2 or more, and a peel displacement of 2.0 mm or less. . JIS K-7181に準じた圧縮強度測定で測定される40%圧縮強度が2MPa以上である請求項1記載の粘着テープ。 2. The pressure-sensitive adhesive tape according to claim 1, which has a 40% compression strength of 2 MPa or more as measured by compression strength measurement according to JIS K-7181. 前記他のポリオレフィン系樹脂が、ポリエチレン系樹脂、ポリプロピレン系樹脂、又はこれらの混合物である請求項に記載の粘着テープ。 2. The pressure-sensitive adhesive tape according to claim 1 , wherein the other polyolefin resin is a polyethylene resin, a polypropylene resin, or a mixture thereof. 前記粘着剤層が粘着付与樹脂を含有しない請求項1記載の粘着テープ。 2. The pressure-sensitive adhesive tape according to claim 1, wherein said pressure-sensitive adhesive layer does not contain a tackifying resin. JIS K7161 2014に準じて測定される前記基材の引張弾性率が30N/mm以上である請求項1に記載の粘着テープ。 The pressure-sensitive adhesive tape according to claim 1, wherein the base material has a tensile modulus of elasticity of 30 N/mm 2 or more as measured according to JIS K7161 2014. 前記基材が独立気泡を含む請求項1に記載の粘着テープ。 2. The pressure-sensitive adhesive tape of claim 1, wherein the substrate contains closed cells. 構造接着用粘着テープである請求項1記載の粘着テープ。 The pressure-sensitive adhesive tape of claim 1, which is a structure-bonding pressure-sensitive adhesive tape. 電子機器接着用粘着テープである請求項1記載の粘着テープ。
The adhesive tape according to claim 1, which is an adhesive tape for bonding electronic equipment.
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